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   <title>Radiopharm reports partial response in RAD204 cancer drug trial</title>
   <link>http://www.streetinsider.com/FDA/Radiopharm+reports+partial+response+in+RAD204+cancer+drug+trial/26798108.html</link>
   <description>

&lt;p&gt;Radiopharm Theranostics (ASX: RAD, NASDAQ: RADX) reported updated clinical results from the third dosing cohort of its Phase 1 trial of RAD204, a PD-L1-targeted lutetium-177 radiotherapeutic being evaluated in patients with advanced solid tumors following prior immunotherapy.&lt;/p&gt;

&lt;p&gt;According to the company, the first patient in cohort three achieved a RECIST-confirmed partial response after the second treatment cycle, with tumor reductions of 19% after dose one, 43% after dose two, 43% after dose three, and 35% after dose four. The patient has remained progression-free beyond seven months across four treatment cycles.&lt;/p&gt;

&lt;p&gt;A second patient in the cohort showed a 7% reduction in target</description>
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   <pubDate>Wed, 22 Jul 2026 07:05:14 -0400</pubDate>
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   <title>Radiopharm reports partial response in RAD204 cancer drug trial</title>
   <link>http://www.streetinsider.com/FDA/Radiopharm+reports+partial+response+in+RAD204+cancer+drug+trial/26798108.html</link>
   <description>

&lt;p&gt;Radiopharm Theranostics (ASX: RAD, NASDAQ: RADX) reported updated clinical results from the third dosing cohort of its Phase 1 trial of RAD204, a PD-L1-targeted lutetium-177 radiotherapeutic being evaluated in patients with advanced solid tumors following prior immunotherapy.&lt;/p&gt;

&lt;p&gt;According to the company, the first patient in cohort three achieved a RECIST-confirmed partial response after the second treatment cycle, with tumor reductions of 19% after dose one, 43% after dose two, 43% after dose three, and 35% after dose four. The patient has remained progression-free beyond seven months across four treatment cycles.&lt;/p&gt;

&lt;p&gt;A second patient in the cohort showed a 7% reduction in target</description>
   <guid isPermaLink="true">http://www.streetinsider.com/FDA/Radiopharm+reports+partial+response+in+RAD204+cancer+drug+trial/26798108.html</guid>
   <pubDate>Wed, 22 Jul 2026 07:05:14 -0400</pubDate>
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   <title>Radiopharm reports partial response in RAD204 cancer drug trial</title>
   <link>http://www.streetinsider.com/FDA/Radiopharm+reports+partial+response+in+RAD204+cancer+drug+trial/26798108.html</link>
   <description>

&lt;p&gt;Radiopharm Theranostics (ASX: RAD, NASDAQ: RADX) reported updated clinical results from the third dosing cohort of its Phase 1 trial of RAD204, a PD-L1-targeted lutetium-177 radiotherapeutic being evaluated in patients with advanced solid tumors following prior immunotherapy.&lt;/p&gt;

&lt;p&gt;According to the company, the first patient in cohort three achieved a RECIST-confirmed partial response after the second treatment cycle, with tumor reductions of 19% after dose one, 43% after dose two, 43% after dose three, and 35% after dose four. The patient has remained progression-free beyond seven months across four treatment cycles.&lt;/p&gt;

&lt;p&gt;A second patient in the cohort showed a 7% reduction in target</description>
   <guid isPermaLink="true">http://www.streetinsider.com/FDA/Radiopharm+reports+partial+response+in+RAD204+cancer+drug+trial/26798108.html</guid>
   <pubDate>Wed, 22 Jul 2026 07:05:14 -0400</pubDate>
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   <title>Radiopharm Theranostics Achieves Confirmed Durable Partial Response in Ongoing Phase 1 Trial of RAD204 in Patients with Advanced Solid Tumors Post-Immunotherapy</title>
   <link>http://www.streetinsider.com/Press+Releases/Radiopharm+Theranostics+Achieves+Confirmed+Durable+Partial+Response+in+Ongoing+Phase+1+Trial+of+RAD204+in+Patients+with+Advanced+Solid+Tumors+Post-Immunotherapy/26798106.html</link>
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&lt;p align=&quot;center&quot;&gt;&lt;em&gt;First RECIST-confirmed durable Partial Response at current highest dose level #3 (90mCi) with the patient remaining progression free beyond seven months&lt;/em&gt;&lt;/p&gt;  &lt;p align=&quot;center&quot;&gt;&lt;em&gt;Second patient dosed remains progression free on treatment with RAD204 with early tumor shrinkage observed after first treatment&lt;/em&gt;&lt;/p&gt;  &lt;p align=&quot;center&quot;&gt;&lt;em&gt;RAD204 is generally well-tolerated with no dose-limiting toxicities observed in any of the dosing cohorts thus far&lt;/em&gt;&lt;/p&gt;  &lt;p&gt;SYDNEY and MALVERN, Pa., July  22, 2026  (GLOBE NEWSWIRE) -- Radiopharm Theranostics (ASX:RAD, Nasdaq: RADX, “Radiopharm” or the “Company”), a clinical-stage biopharmaceutical company focused on developing innovative oncology radiopharmaceuticals for areas of high unmet medical need,</description>
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   <pubDate>Wed, 22 Jul 2026 07:05:00 -0400</pubDate>
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   <title>Radiopharm Theranostics Achieves Confirmed Durable Partial Response in Ongoing Phase 1 Trial of RAD204 in Patients with Advanced Solid Tumors Post-Immunotherapy</title>
   <link>http://www.streetinsider.com/Press+Releases/Radiopharm+Theranostics+Achieves+Confirmed+Durable+Partial+Response+in+Ongoing+Phase+1+Trial+of+RAD204+in+Patients+with+Advanced+Solid+Tumors+Post-Immunotherapy/26798106.html</link>
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&lt;p align=&quot;center&quot;&gt;&lt;em&gt;First RECIST-confirmed durable Partial Response at current highest dose level #3 (90mCi) with the patient remaining progression free beyond seven months&lt;/em&gt;&lt;/p&gt;  &lt;p align=&quot;center&quot;&gt;&lt;em&gt;Second patient dosed remains progression free on treatment with RAD204 with early tumor shrinkage observed after first treatment&lt;/em&gt;&lt;/p&gt;  &lt;p align=&quot;center&quot;&gt;&lt;em&gt;RAD204 is generally well-tolerated with no dose-limiting toxicities observed in any of the dosing cohorts thus far&lt;/em&gt;&lt;/p&gt;  &lt;p&gt;SYDNEY and MALVERN, Pa., July  22, 2026  (GLOBE NEWSWIRE) -- Radiopharm Theranostics (ASX:RAD, Nasdaq: RADX, “Radiopharm” or the “Company”), a clinical-stage biopharmaceutical company focused on developing innovative oncology radiopharmaceuticals for areas of high unmet medical need,</description>
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   <pubDate>Wed, 22 Jul 2026 07:05:00 -0400</pubDate>
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   <title>Radiopharm Theranostics Achieves Confirmed Durable Partial Response in Ongoing Phase 1 Trial of RAD204 in Patients with Advanced Solid Tumors Post-Immunotherapy</title>
   <link>http://www.streetinsider.com/Press+Releases/Radiopharm+Theranostics+Achieves+Confirmed+Durable+Partial+Response+in+Ongoing+Phase+1+Trial+of+RAD204+in+Patients+with+Advanced+Solid+Tumors+Post-Immunotherapy/26798106.html</link>
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&lt;p align=&quot;center&quot;&gt;&lt;em&gt;First RECIST-confirmed durable Partial Response at current highest dose level #3 (90mCi) with the patient remaining progression free beyond seven months&lt;/em&gt;&lt;/p&gt;  &lt;p align=&quot;center&quot;&gt;&lt;em&gt;Second patient dosed remains progression free on treatment with RAD204 with early tumor shrinkage observed after first treatment&lt;/em&gt;&lt;/p&gt;  &lt;p align=&quot;center&quot;&gt;&lt;em&gt;RAD204 is generally well-tolerated with no dose-limiting toxicities observed in any of the dosing cohorts thus far&lt;/em&gt;&lt;/p&gt;  &lt;p&gt;SYDNEY and MALVERN, Pa., July  22, 2026  (GLOBE NEWSWIRE) -- Radiopharm Theranostics (ASX:RAD, Nasdaq: RADX, “Radiopharm” or the “Company”), a clinical-stage biopharmaceutical company focused on developing innovative oncology radiopharmaceuticals for areas of high unmet medical need,</description>
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   <pubDate>Wed, 22 Jul 2026 07:05:00 -0400</pubDate>
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   <title>Radiopharm Theranostics Achieves Confirmed Durable Partial Response in Ongoing Phase 1 Trial of RAD204 in Patients with Advanced Solid Tumors Post-Immunotherapy</title>
   <link>http://www.streetinsider.com/Globe+Newswire/Radiopharm+Theranostics+Achieves+Confirmed+Durable+Partial+Response+in+Ongoing+Phase+1+Trial+of+RAD204+in+Patients+with+Advanced+Solid+Tumors+Post-Immunotherapy/26798106.html</link>
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&lt;p align=&quot;center&quot;&gt;&lt;em&gt;First RECIST-confirmed durable Partial Response at current highest dose level #3 (90mCi) with the patient remaining progression free beyond seven months&lt;/em&gt;&lt;/p&gt;  &lt;p align=&quot;center&quot;&gt;&lt;em&gt;Second patient dosed remains progression free on treatment with RAD204 with early tumor shrinkage observed after first treatment&lt;/em&gt;&lt;/p&gt;  &lt;p align=&quot;center&quot;&gt;&lt;em&gt;RAD204 is generally well-tolerated with no dose-limiting toxicities observed in any of the dosing cohorts thus far&lt;/em&gt;&lt;/p&gt;  &lt;p&gt;SYDNEY and MALVERN, Pa., July  22, 2026  (GLOBE NEWSWIRE) -- Radiopharm Theranostics (ASX:RAD, Nasdaq: RADX, “Radiopharm” or the “Company”), a clinical-stage biopharmaceutical company focused on developing innovative oncology radiopharmaceuticals for areas of high unmet medical need,</description>
   <guid isPermaLink="true">http://www.streetinsider.com/Globe+Newswire/Radiopharm+Theranostics+Achieves+Confirmed+Durable+Partial+Response+in+Ongoing+Phase+1+Trial+of+RAD204+in+Patients+with+Advanced+Solid+Tumors+Post-Immunotherapy/26798106.html</guid>
   <pubDate>Wed, 22 Jul 2026 07:05:00 -0400</pubDate>
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   <title>Radiopharm Theranostics Achieves Confirmed Durable Partial Response in Ongoing Phase 1 Trial of RAD204 in Patients with Advanced Solid Tumors Post-Immunotherapy</title>
   <link>http://www.streetinsider.com/Globe+Newswire/Radiopharm+Theranostics+Achieves+Confirmed+Durable+Partial+Response+in+Ongoing+Phase+1+Trial+of+RAD204+in+Patients+with+Advanced+Solid+Tumors+Post-Immunotherapy/26798106.html</link>
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&lt;p align=&quot;center&quot;&gt;&lt;em&gt;First RECIST-confirmed durable Partial Response at current highest dose level #3 (90mCi) with the patient remaining progression free beyond seven months&lt;/em&gt;&lt;/p&gt;  &lt;p align=&quot;center&quot;&gt;&lt;em&gt;Second patient dosed remains progression free on treatment with RAD204 with early tumor shrinkage observed after first treatment&lt;/em&gt;&lt;/p&gt;  &lt;p align=&quot;center&quot;&gt;&lt;em&gt;RAD204 is generally well-tolerated with no dose-limiting toxicities observed in any of the dosing cohorts thus far&lt;/em&gt;&lt;/p&gt;  &lt;p&gt;SYDNEY and MALVERN, Pa., July  22, 2026  (GLOBE NEWSWIRE) -- Radiopharm Theranostics (ASX:RAD, Nasdaq: RADX, “Radiopharm” or the “Company”), a clinical-stage biopharmaceutical company focused on developing innovative oncology radiopharmaceuticals for areas of high unmet medical need,</description>
   <guid isPermaLink="true">http://www.streetinsider.com/Globe+Newswire/Radiopharm+Theranostics+Achieves+Confirmed+Durable+Partial+Response+in+Ongoing+Phase+1+Trial+of+RAD204+in+Patients+with+Advanced+Solid+Tumors+Post-Immunotherapy/26798106.html</guid>
   <pubDate>Wed, 22 Jul 2026 07:05:00 -0400</pubDate>
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   <title>Radiopharm Theranostics Achieves Confirmed Durable Partial Response in Ongoing Phase 1 Trial of RAD204 in Patients with Advanced Solid Tumors Post-Immunotherapy</title>
   <link>http://www.streetinsider.com/Globe+Newswire/Radiopharm+Theranostics+Achieves+Confirmed+Durable+Partial+Response+in+Ongoing+Phase+1+Trial+of+RAD204+in+Patients+with+Advanced+Solid+Tumors+Post-Immunotherapy/26798106.html</link>
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&lt;p align=&quot;center&quot;&gt;&lt;em&gt;First RECIST-confirmed durable Partial Response at current highest dose level #3 (90mCi) with the patient remaining progression free beyond seven months&lt;/em&gt;&lt;/p&gt;  &lt;p align=&quot;center&quot;&gt;&lt;em&gt;Second patient dosed remains progression free on treatment with RAD204 with early tumor shrinkage observed after first treatment&lt;/em&gt;&lt;/p&gt;  &lt;p align=&quot;center&quot;&gt;&lt;em&gt;RAD204 is generally well-tolerated with no dose-limiting toxicities observed in any of the dosing cohorts thus far&lt;/em&gt;&lt;/p&gt;  &lt;p&gt;SYDNEY and MALVERN, Pa., July  22, 2026  (GLOBE NEWSWIRE) -- Radiopharm Theranostics (ASX:RAD, Nasdaq: RADX, “Radiopharm” or the “Company”), a clinical-stage biopharmaceutical company focused on developing innovative oncology radiopharmaceuticals for areas of high unmet medical need,</description>
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   <pubDate>Wed, 22 Jul 2026 07:05:00 -0400</pubDate>
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   <title>Radiopharm RAD101 meets Phase 2b endpoint for brain metastases</title>
   <link>http://www.streetinsider.com/FDA/Radiopharm+RAD101+meets+Phase+2b+endpoint+for+brain+metastases/26798039.html</link>
   <description>

&lt;p&gt;Radiopharm Theranostics (ASX: RAD, NASDAQ: RADX) reported that its RAD101 imaging agent met the primary endpoint of a Phase 2b clinical trial, showing 93% concordance between PET and MRI imaging across all evaluable lesions in patients with suspected recurrent brain metastases.&lt;/p&gt;

&lt;p&gt;The U.S. multicenter, open-label, single-arm trial enrolled 30 evaluable patients with suspected recurrence of brain metastases from solid tumors following stereotactic radiosurgery. Among 14 patients with available six-month follow-up and biopsy data, preliminary sensitivity — the ability to correctly identify patients with disease — was 86%. Specificity data is expected in the fourth quarter of 2026.&lt;/p&gt;

&lt;p&gt;RAD101 is a small molecule</description>
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   <title>Radiopharm RAD101 meets Phase 2b endpoint for brain metastases</title>
   <link>http://www.streetinsider.com/FDA/Radiopharm+RAD101+meets+Phase+2b+endpoint+for+brain+metastases/26798039.html</link>
   <description>

&lt;p&gt;Radiopharm Theranostics (ASX: RAD, NASDAQ: RADX) reported that its RAD101 imaging agent met the primary endpoint of a Phase 2b clinical trial, showing 93% concordance between PET and MRI imaging across all evaluable lesions in patients with suspected recurrent brain metastases.&lt;/p&gt;

&lt;p&gt;The U.S. multicenter, open-label, single-arm trial enrolled 30 evaluable patients with suspected recurrence of brain metastases from solid tumors following stereotactic radiosurgery. Among 14 patients with available six-month follow-up and biopsy data, preliminary sensitivity — the ability to correctly identify patients with disease — was 86%. Specificity data is expected in the fourth quarter of 2026.&lt;/p&gt;

&lt;p&gt;RAD101 is a small molecule</description>
   <guid isPermaLink="true">http://www.streetinsider.com/FDA/Radiopharm+RAD101+meets+Phase+2b+endpoint+for+brain+metastases/26798039.html</guid>
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   <title>Radiopharm RAD101 meets Phase 2b endpoint for brain metastases</title>
   <link>http://www.streetinsider.com/FDA/Radiopharm+RAD101+meets+Phase+2b+endpoint+for+brain+metastases/26798039.html</link>
   <description>

&lt;p&gt;Radiopharm Theranostics (ASX: RAD, NASDAQ: RADX) reported that its RAD101 imaging agent met the primary endpoint of a Phase 2b clinical trial, showing 93% concordance between PET and MRI imaging across all evaluable lesions in patients with suspected recurrent brain metastases.&lt;/p&gt;

&lt;p&gt;The U.S. multicenter, open-label, single-arm trial enrolled 30 evaluable patients with suspected recurrence of brain metastases from solid tumors following stereotactic radiosurgery. Among 14 patients with available six-month follow-up and biopsy data, preliminary sensitivity — the ability to correctly identify patients with disease — was 86%. Specificity data is expected in the fourth quarter of 2026.&lt;/p&gt;

&lt;p&gt;RAD101 is a small molecule</description>
   <guid isPermaLink="true">http://www.streetinsider.com/FDA/Radiopharm+RAD101+meets+Phase+2b+endpoint+for+brain+metastases/26798039.html</guid>
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   <title>Radiopharm RAD101 meets Phase 2b endpoint for brain metastases</title>
   <link>http://www.streetinsider.com/FDA/Radiopharm+RAD101+meets+Phase+2b+endpoint+for+brain+metastases/26798039.html</link>
   <description>

&lt;p&gt;Radiopharm Theranostics (ASX: RAD, NASDAQ: RADX) reported that its RAD101 imaging agent met the primary endpoint of a Phase 2b clinical trial, showing 93% concordance between PET and MRI imaging across all evaluable lesions in patients with suspected recurrent brain metastases.&lt;/p&gt;

&lt;p&gt;The U.S. multicenter, open-label, single-arm trial enrolled 30 evaluable patients with suspected recurrence of brain metastases from solid tumors following stereotactic radiosurgery. Among 14 patients with available six-month follow-up and biopsy data, preliminary sensitivity — the ability to correctly identify patients with disease — was 86%. Specificity data is expected in the fourth quarter of 2026.&lt;/p&gt;

&lt;p&gt;RAD101 is a small molecule</description>
   <guid isPermaLink="true">http://www.streetinsider.com/FDA/Radiopharm+RAD101+meets+Phase+2b+endpoint+for+brain+metastases/26798039.html</guid>
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   <title>Radiopharm RAD101 meets Phase 2b endpoint for brain metastases</title>
   <link>http://www.streetinsider.com/FDA/Radiopharm+RAD101+meets+Phase+2b+endpoint+for+brain+metastases/26798039.html</link>
   <description>

&lt;p&gt;Radiopharm Theranostics (ASX: RAD, NASDAQ: RADX) reported that its RAD101 imaging agent met the primary endpoint of a Phase 2b clinical trial, showing 93% concordance between PET and MRI imaging across all evaluable lesions in patients with suspected recurrent brain metastases.&lt;/p&gt;

&lt;p&gt;The U.S. multicenter, open-label, single-arm trial enrolled 30 evaluable patients with suspected recurrence of brain metastases from solid tumors following stereotactic radiosurgery. Among 14 patients with available six-month follow-up and biopsy data, preliminary sensitivity — the ability to correctly identify patients with disease — was 86%. Specificity data is expected in the fourth quarter of 2026.&lt;/p&gt;

&lt;p&gt;RAD101 is a small molecule</description>
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   <title>Radiopharm RAD101 meets Phase 2b endpoint for brain metastases</title>
   <link>http://www.streetinsider.com/FDA/Radiopharm+RAD101+meets+Phase+2b+endpoint+for+brain+metastases/26798039.html</link>
   <description>

&lt;p&gt;Radiopharm Theranostics (ASX: RAD, NASDAQ: RADX) reported that its RAD101 imaging agent met the primary endpoint of a Phase 2b clinical trial, showing 93% concordance between PET and MRI imaging across all evaluable lesions in patients with suspected recurrent brain metastases.&lt;/p&gt;

&lt;p&gt;The U.S. multicenter, open-label, single-arm trial enrolled 30 evaluable patients with suspected recurrence of brain metastases from solid tumors following stereotactic radiosurgery. Among 14 patients with available six-month follow-up and biopsy data, preliminary sensitivity — the ability to correctly identify patients with disease — was 86%. Specificity data is expected in the fourth quarter of 2026.&lt;/p&gt;

&lt;p&gt;RAD101 is a small molecule</description>
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   <title>Radiopharm RAD101 meets Phase 2b endpoint for brain metastases</title>
   <link>http://www.streetinsider.com/FDA/Radiopharm+RAD101+meets+Phase+2b+endpoint+for+brain+metastases/26798039.html</link>
   <description>

&lt;p&gt;Radiopharm Theranostics (ASX: RAD, NASDAQ: RADX) reported that its RAD101 imaging agent met the primary endpoint of a Phase 2b clinical trial, showing 93% concordance between PET and MRI imaging across all evaluable lesions in patients with suspected recurrent brain metastases.&lt;/p&gt;

&lt;p&gt;The U.S. multicenter, open-label, single-arm trial enrolled 30 evaluable patients with suspected recurrence of brain metastases from solid tumors following stereotactic radiosurgery. Among 14 patients with available six-month follow-up and biopsy data, preliminary sensitivity — the ability to correctly identify patients with disease — was 86%. Specificity data is expected in the fourth quarter of 2026.&lt;/p&gt;

&lt;p&gt;RAD101 is a small molecule</description>
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   <title>Radiopharm Theranostics Announces Positive Phase 2b Trial Results of RAD 101 for Diagnosis of Brain Metastases</title>
   <link>http://www.streetinsider.com/Press+Releases/Radiopharm+Theranostics+Announces+Positive+Phase+2b+Trial+Results+of+RAD+101+for+Diagnosis+of+Brain+Metastases/26797975.html</link>
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&lt;p align=&quot;center&quot;&gt;&lt;em&gt;RAD101 PET demonstrated 93% concordance with MRI across all evaluable lesions, meeting the trial&amp;apos;s primary endpoint.&lt;/em&gt;&lt;/p&gt;  &lt;p align=&quot;center&quot;&gt;&lt;em&gt;14 patients with available data from six-month follow-up and biopsy show preliminary 86% (12/14) Sensitivity (secondary objective). Specificity data will be available in Q4 2026.&lt;/em&gt;&lt;/p&gt;  &lt;p align=&quot;center&quot;&gt;&lt;em&gt;The Company plans to advance RAD101 into a U.S. Phase 3 pivotal trial in Q4 2026&lt;/em&gt;&lt;/p&gt;  &lt;p align=&quot;center&quot;&gt;&lt;em&gt;The imaging Brain Metastases total addressable market is ~$600+m for which there is no currently approved PET product&lt;/em&gt;&lt;/p&gt;  &lt;p&gt;SYDNEY, July  22, 2026  (GLOBE NEWSWIRE) -- Radiopharm Theranostics (ASX:RAD, “Radiopharm” or the “Company”), a</description>
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   <title>Radiopharm Theranostics Announces Positive Phase 2b Trial Results of RAD 101 for Diagnosis of Brain Metastases</title>
   <link>http://www.streetinsider.com/Press+Releases/Radiopharm+Theranostics+Announces+Positive+Phase+2b+Trial+Results+of+RAD+101+for+Diagnosis+of+Brain+Metastases/26797975.html</link>
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&lt;p align=&quot;center&quot;&gt;&lt;em&gt;RAD101 PET demonstrated 93% concordance with MRI across all evaluable lesions, meeting the trial&amp;apos;s primary endpoint.&lt;/em&gt;&lt;/p&gt;  &lt;p align=&quot;center&quot;&gt;&lt;em&gt;14 patients with available data from six-month follow-up and biopsy show preliminary 86% (12/14) Sensitivity (secondary objective). Specificity data will be available in Q4 2026.&lt;/em&gt;&lt;/p&gt;  &lt;p align=&quot;center&quot;&gt;&lt;em&gt;The Company plans to advance RAD101 into a U.S. Phase 3 pivotal trial in Q4 2026&lt;/em&gt;&lt;/p&gt;  &lt;p align=&quot;center&quot;&gt;&lt;em&gt;The imaging Brain Metastases total addressable market is ~$600+m for which there is no currently approved PET product&lt;/em&gt;&lt;/p&gt;  &lt;p&gt;SYDNEY, July  22, 2026  (GLOBE NEWSWIRE) -- Radiopharm Theranostics (ASX:RAD, “Radiopharm” or the “Company”), a</description>
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   <title>Radiopharm Theranostics Announces Positive Phase 2b Trial Results of RAD 101 for Diagnosis of Brain Metastases</title>
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&lt;p align=&quot;center&quot;&gt;&lt;em&gt;RAD101 PET demonstrated 93% concordance with MRI across all evaluable lesions, meeting the trial&amp;apos;s primary endpoint.&lt;/em&gt;&lt;/p&gt;  &lt;p align=&quot;center&quot;&gt;&lt;em&gt;14 patients with available data from six-month follow-up and biopsy show preliminary 86% (12/14) Sensitivity (secondary objective). Specificity data will be available in Q4 2026.&lt;/em&gt;&lt;/p&gt;  &lt;p align=&quot;center&quot;&gt;&lt;em&gt;The Company plans to advance RAD101 into a U.S. Phase 3 pivotal trial in Q4 2026&lt;/em&gt;&lt;/p&gt;  &lt;p align=&quot;center&quot;&gt;&lt;em&gt;The imaging Brain Metastases total addressable market is ~$600+m for which there is no currently approved PET product&lt;/em&gt;&lt;/p&gt;  &lt;p&gt;SYDNEY, July  22, 2026  (GLOBE NEWSWIRE) -- Radiopharm Theranostics (ASX:RAD, “Radiopharm” or the “Company”), a</description>
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   <title>Radiopharm Theranostics Announces Positive Phase 2b Trial Results of RAD 101 for Diagnosis of Brain Metastases</title>
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&lt;p align=&quot;center&quot;&gt;&lt;em&gt;RAD101 PET demonstrated 93% concordance with MRI across all evaluable lesions, meeting the trial&amp;apos;s primary endpoint.&lt;/em&gt;&lt;/p&gt;  &lt;p align=&quot;center&quot;&gt;&lt;em&gt;14 patients with available data from six-month follow-up and biopsy show preliminary 86% (12/14) Sensitivity (secondary objective). Specificity data will be available in Q4 2026.&lt;/em&gt;&lt;/p&gt;  &lt;p align=&quot;center&quot;&gt;&lt;em&gt;The Company plans to advance RAD101 into a U.S. Phase 3 pivotal trial in Q4 2026&lt;/em&gt;&lt;/p&gt;  &lt;p align=&quot;center&quot;&gt;&lt;em&gt;The imaging Brain Metastases total addressable market is ~$600+m for which there is no currently approved PET product&lt;/em&gt;&lt;/p&gt;  &lt;p&gt;SYDNEY, July  22, 2026  (GLOBE NEWSWIRE) -- Radiopharm Theranostics (ASX:RAD, “Radiopharm” or the “Company”), a</description>
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   <title>Radiopharm Theranostics Announces Positive Phase 2b Trial Results of RAD 101 for Diagnosis of Brain Metastases</title>
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&lt;p align=&quot;center&quot;&gt;&lt;em&gt;RAD101 PET demonstrated 93% concordance with MRI across all evaluable lesions, meeting the trial&amp;apos;s primary endpoint.&lt;/em&gt;&lt;/p&gt;  &lt;p align=&quot;center&quot;&gt;&lt;em&gt;14 patients with available data from six-month follow-up and biopsy show preliminary 86% (12/14) Sensitivity (secondary objective). Specificity data will be available in Q4 2026.&lt;/em&gt;&lt;/p&gt;  &lt;p align=&quot;center&quot;&gt;&lt;em&gt;The Company plans to advance RAD101 into a U.S. Phase 3 pivotal trial in Q4 2026&lt;/em&gt;&lt;/p&gt;  &lt;p align=&quot;center&quot;&gt;&lt;em&gt;The imaging Brain Metastases total addressable market is ~$600+m for which there is no currently approved PET product&lt;/em&gt;&lt;/p&gt;  &lt;p&gt;SYDNEY, July  22, 2026  (GLOBE NEWSWIRE) -- Radiopharm Theranostics (ASX:RAD, “Radiopharm” or the “Company”), a</description>
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   <title>Radiopharm Theranostics Announces Positive Phase 2b Trial Results of RAD 101 for Diagnosis of Brain Metastases</title>
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&lt;p align=&quot;center&quot;&gt;&lt;em&gt;RAD101 PET demonstrated 93% concordance with MRI across all evaluable lesions, meeting the trial&amp;apos;s primary endpoint.&lt;/em&gt;&lt;/p&gt;  &lt;p align=&quot;center&quot;&gt;&lt;em&gt;14 patients with available data from six-month follow-up and biopsy show preliminary 86% (12/14) Sensitivity (secondary objective). Specificity data will be available in Q4 2026.&lt;/em&gt;&lt;/p&gt;  &lt;p align=&quot;center&quot;&gt;&lt;em&gt;The Company plans to advance RAD101 into a U.S. Phase 3 pivotal trial in Q4 2026&lt;/em&gt;&lt;/p&gt;  &lt;p align=&quot;center&quot;&gt;&lt;em&gt;The imaging Brain Metastases total addressable market is ~$600+m for which there is no currently approved PET product&lt;/em&gt;&lt;/p&gt;  &lt;p&gt;SYDNEY, July  22, 2026  (GLOBE NEWSWIRE) -- Radiopharm Theranostics (ASX:RAD, “Radiopharm” or the “Company”), a</description>
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   <title>Radiopharm Theranostics Announces Positive Phase 2b Trial Results of RAD 101 for Diagnosis of Brain Metastases</title>
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&lt;p align=&quot;center&quot;&gt;&lt;em&gt;RAD101 PET demonstrated 93% concordance with MRI across all evaluable lesions, meeting the trial&amp;apos;s primary endpoint.&lt;/em&gt;&lt;/p&gt;  &lt;p align=&quot;center&quot;&gt;&lt;em&gt;14 patients with available data from six-month follow-up and biopsy show preliminary 86% (12/14) Sensitivity (secondary objective). Specificity data will be available in Q4 2026.&lt;/em&gt;&lt;/p&gt;  &lt;p align=&quot;center&quot;&gt;&lt;em&gt;The Company plans to advance RAD101 into a U.S. Phase 3 pivotal trial in Q4 2026&lt;/em&gt;&lt;/p&gt;  &lt;p align=&quot;center&quot;&gt;&lt;em&gt;The imaging Brain Metastases total addressable market is ~$600+m for which there is no currently approved PET product&lt;/em&gt;&lt;/p&gt;  &lt;p&gt;SYDNEY, July  22, 2026  (GLOBE NEWSWIRE) -- Radiopharm Theranostics (ASX:RAD, “Radiopharm” or the “Company”), a</description>
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&lt;p align=&quot;center&quot;&gt;&lt;em&gt;RAD101 PET demonstrated 93% concordance with MRI across all evaluable lesions, meeting the trial&amp;apos;s primary endpoint.&lt;/em&gt;&lt;/p&gt;  &lt;p align=&quot;center&quot;&gt;&lt;em&gt;14 patients with available data from six-month follow-up and biopsy show preliminary 86% (12/14) Sensitivity (secondary objective). Specificity data will be available in Q4 2026.&lt;/em&gt;&lt;/p&gt;  &lt;p align=&quot;center&quot;&gt;&lt;em&gt;The Company plans to advance RAD101 into a U.S. Phase 3 pivotal trial in Q4 2026&lt;/em&gt;&lt;/p&gt;  &lt;p align=&quot;center&quot;&gt;&lt;em&gt;The imaging Brain Metastases total addressable market is ~$600+m for which there is no currently approved PET product&lt;/em&gt;&lt;/p&gt;  &lt;p&gt;SYDNEY, July  22, 2026  (GLOBE NEWSWIRE) -- Radiopharm Theranostics (ASX:RAD, “Radiopharm” or the “Company”), a</description>
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   <title>Radiopharm Theranostics Announces Positive Phase 2b Trial Results of RAD 101 for Diagnosis of Brain Metastases</title>
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&lt;p align=&quot;center&quot;&gt;&lt;em&gt;RAD101 PET demonstrated 93% concordance with MRI across all evaluable lesions, meeting the trial&amp;apos;s primary endpoint.&lt;/em&gt;&lt;/p&gt;  &lt;p align=&quot;center&quot;&gt;&lt;em&gt;14 patients with available data from six-month follow-up and biopsy show preliminary 86% (12/14) Sensitivity (secondary objective). Specificity data will be available in Q4 2026.&lt;/em&gt;&lt;/p&gt;  &lt;p align=&quot;center&quot;&gt;&lt;em&gt;The Company plans to advance RAD101 into a U.S. Phase 3 pivotal trial in Q4 2026&lt;/em&gt;&lt;/p&gt;  &lt;p align=&quot;center&quot;&gt;&lt;em&gt;The imaging Brain Metastases total addressable market is ~$600+m for which there is no currently approved PET product&lt;/em&gt;&lt;/p&gt;  &lt;p&gt;SYDNEY, July  22, 2026  (GLOBE NEWSWIRE) -- Radiopharm Theranostics (ASX:RAD, “Radiopharm” or the “Company”), a</description>
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   <pubDate>Wed, 22 Jul 2026 07:00:00 -0400</pubDate>
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